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1.
Br J Cancer ; 104(1): 83-90, 2011 Jan 04.
Artigo em Inglês | MEDLINE | ID: mdl-21139581

RESUMO

BACKGROUND: Progressive tumour growth is dependent on the development of a functional tumour vasculature and highly regulated by growth factors and cytokines. Nitric oxide (NO) is a free radical, produced both by tumour and host cells, and functions as a signalling molecule downstream of several angiogenic factors. Both pro- and antitumourigenic properties have been attributed to NO. METHODS: The expression of the inducible isoform of NO synthase (iNOS) was knocked down in the C6 glioma cell line using constitutive expression of antisense RNA, and the effect of tumour-derived NO on tumour progression and angiogenesis was investigated. RESULTS: Tumours in which iNOS expression was decreased displayed significantly reduced growth rates compared with tumours derived from parental C6 cells. Quantitative non-invasive magnetic resonance imaging and fluorescence microscopy of tumour uptake of Hoechst 33342, and haematoxylin and eosin staining, revealed significantly impaired vascular development and function in antisense iNOS tumours compared with control in vivo, primarily associated with the more necrotic tumour core. Decreased iNOS expression had no effect on tumour VEGF expression. CONCLUSION: Nitric oxide derived from tumour iNOS is an important modulator of tumour progression and angiogenesis in C6 gliomas and further supports the therapeutic strategy of inhibiting iNOS for the treatment of cancer.


Assuntos
Neoplasias Encefálicas/irrigação sanguínea , Neoplasias Encefálicas/enzimologia , Glioma/irrigação sanguínea , Glioma/enzimologia , Neovascularização Patológica/enzimologia , Óxido Nítrico Sintase Tipo II/fisiologia , Animais , Western Blotting , Neoplasias Encefálicas/patologia , DNA Antissenso/farmacologia , Progressão da Doença , Feminino , Inativação Gênica/fisiologia , Glioma/patologia , Técnicas Imunoenzimáticas , Imageamento por Ressonância Magnética , Camundongos , Camundongos Nus , Microscopia de Fluorescência , Óxido Nítrico/metabolismo , Ratos , Células Tumorais Cultivadas , Fator A de Crescimento do Endotélio Vascular/metabolismo , Ensaios Antitumorais Modelo de Xenoenxerto
2.
Dev Med Child Neurol ; 41(10): 676-82, 1999 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-10587044

RESUMO

The repeatability of energy-expenditure measurements were studied in five children and four adults without disabilities using the Cosmed K4 (high technology). The ability to detect change in measurements was compared between this instrument and the Physiological Cost Index (PCI; low technology). The results of repeatability (95% range) for oxygen cost were 13.1% in children and 13% in adults. In contrast, the SD of PCI was 6 to 72% of the mean in adults and wider in children (91%; 95% range). The validity of PCI as an outcome measure was questioned. In addition, 177 children with motor disability were prospectively studied using the Cosmed K4. Previous experience with the Cosmed K2 (intermediate technology) helped to develop a practical and repeatable protocol for testing children with disability using the Cosmed K4. The protocol commenced with 5 minutes of rest to achieve baseline values of heart rate and oxygen consumption, followed by 10 minutes of continuous walking at a self-selected speed on a 10-metre level oval walking track. The test concluded with 5 minutes of rest to monitor the return to baseline values. Ninety-one percent of the children with disability quickly reached a steady-state of oxygen consumption and carbon-dioxide production. The carbon-dioxide sensor in the Cosmed K4 has enabled a new group of severely involved children with cerebral palsy (9%) to be defined. These children have been termed 'physiologically marginal ambulators'.


Assuntos
Pessoas com Deficiência , Metabolismo Energético , Marcha , Adulto , Criança , Pré-Escolar , Feminino , Frequência Cardíaca , Humanos , Masculino , Consumo de Oxigênio , Valores de Referência , Reprodutibilidade dos Testes
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